Identity
- Trade Name
- VILET FDA UDI
- Generic Name
- Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
- Device Name
- SUTURE FDA UDI
- Model / Reference
- V570 FDA UDI
- Description
- SUTURE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00812444026054 FDA UDI
- FDA Product Code
- GAM FDA UDI
- GMDN Term
- Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4493 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Polyester suture, bioabsorbable, multifilament, non-antimicrobial
Vilet by Riverpoint Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Coated VICRYL — Ethicon Inc. · Class II
- DemeSORB — DemeTECH Corp · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Riverpoint Medical Llc
Sources (1)
- FDA UDI 0a69d4f2-1e8b-45b1-a8ff-a4c75645cbfe 33 fields · synced Jun 7, 2026